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Circulation Research. 1998;82:306-313

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(Circulation Research. 1998;82:306-313.)
© 1998 American Heart Association, Inc.


Point/Counterpoint

Gene Therapy for Restenosis

Are We Ready?

Mary Beth DeYoung, , David A. Dichek

From the Gladstone Institute of Cardiovascular Disease and Department of Medicine, University of California, San Francisco.

Correspondence to David Dichek, MD, Gladstone Institute of Cardiovascular Disease, PO Box 419100, San Francisco, CA 94141-9100. E-mail david_dichek{at}quickmail.ucsf.edu

Abstract—The application of gene therapy techniques to the clinical problem of coronary restenosis has generated tremendous attention and enthusiasm. Use of gene transfer technology to prevent a common intractable illness would represent a watershed event for human gene therapy. However, the time is not yet right to initiate gene therapy trials for restenosis. The biology of restenosis is incompletely understood, catheter-based gene delivery is poorly adapted to the coronary circulation, and current gene transfer vectors are ill-suited for safe and effective gene delivery to the coronary artery wall. Basic research designed to overcome these obstacles is currently more appropriate than the initiation of clinical trials.


Key Words: gene therapy • restenosis • adenovirus




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